TY - JOUR
T1 - Transcranial magnetic stimulation of degenerating brain
T2 - A comparison of normal aging, Alzheimer's, Parkinson's and Huntington's disease
AU - Ljubisavljevic, M. R.
AU - Ismail, F. Y.
AU - Filipovic, S.
PY - 2013/1/1
Y1 - 2013/1/1
N2 - Although the brain's ability to change constantly in response to external and internal inputs is now well recognized the mechanisms behind it in normal aging and neurodegeneration are less well understood. To gain a better understanding, transcranial magnetic stimulation (TMS) has been used extensively to characterize non-invasively the cortical neurophysiology of the aging and degenerating brain. Furthermore, there has been a surge of studies examining whether repetitive TMS (rTMS) can be used to improve functional deficits in various conditions including normal aging, Alzheimer's and Parkinson's disease. The results of these studies in normal aging and neurodegeneration have emerged reasonably coherent in delineating the main pathology in spite of considerable technical limitations, omnipresent methodological variability, and extraordinary patient heterogeneity. Nevertheless, comparing and integrating what is known about TMS measurements of cortical excitability and plasticity in disorders that predominantly affect cortical brain structures with disorders that predominantly affect subcortical brain structures may provide better understanding of normal and abnormal brain aging fostering new. The present review provides a TMS perspective of changes in cortical neurophysiology and neurochemistry in normal aging and neurodegeneration by integrating what is revealed in individual TMS measurements of cortical excitability and plasticity in physiological aging, Alzheimer's, Parkinson's, and Huntington's, disease. The paper also reflects on current developments in utilizing TMS as a physiologic biomarker to discriminate physiologic aging from neurodegeneration and its potential as a method of therapeutic intervention.
AB - Although the brain's ability to change constantly in response to external and internal inputs is now well recognized the mechanisms behind it in normal aging and neurodegeneration are less well understood. To gain a better understanding, transcranial magnetic stimulation (TMS) has been used extensively to characterize non-invasively the cortical neurophysiology of the aging and degenerating brain. Furthermore, there has been a surge of studies examining whether repetitive TMS (rTMS) can be used to improve functional deficits in various conditions including normal aging, Alzheimer's and Parkinson's disease. The results of these studies in normal aging and neurodegeneration have emerged reasonably coherent in delineating the main pathology in spite of considerable technical limitations, omnipresent methodological variability, and extraordinary patient heterogeneity. Nevertheless, comparing and integrating what is known about TMS measurements of cortical excitability and plasticity in disorders that predominantly affect cortical brain structures with disorders that predominantly affect subcortical brain structures may provide better understanding of normal and abnormal brain aging fostering new. The present review provides a TMS perspective of changes in cortical neurophysiology and neurochemistry in normal aging and neurodegeneration by integrating what is revealed in individual TMS measurements of cortical excitability and plasticity in physiological aging, Alzheimer's, Parkinson's, and Huntington's, disease. The paper also reflects on current developments in utilizing TMS as a physiologic biomarker to discriminate physiologic aging from neurodegeneration and its potential as a method of therapeutic intervention.
KW - Alzheimer's disease
KW - Cortical plasticity
KW - Cortical reactivity
KW - Huntington's disease
KW - Neurodegeneration
KW - Normal aging
KW - Parkinson's disease
KW - Transcranial magnetic stimulation
UR - http://www.scopus.com/inward/record.url?scp=84882739781&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84882739781&partnerID=8YFLogxK
U2 - 10.2174/15672050113109990133
DO - 10.2174/15672050113109990133
M3 - Review article
C2 - 23627752
AN - SCOPUS:84882739781
SN - 1567-2050
VL - 10
SP - 578
EP - 596
JO - Current Alzheimer Research
JF - Current Alzheimer Research
IS - 6
ER -